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nucleophile
(redirected from Nucleophilicity)

   Also found in: Dictionary/thesaurus, Medical, Wikipedia 0.01 sec.

nucleophile

Atom or molecule that contains an electron pair available for bonding and in chemical reactions therefore seeks a positive centre, such as the nucleus of an atom or the positive end of a polar molecule (see covalent bond; electric dipole). In the Lewis electron theory (see acid-base theory), advanced by the U.S. chemist Gilbert Lewis (1875–1946) in 1923, nucleophiles are by definition Lewis bases. Examples include the hydroxide ion (OH), the ions of the halogens chlorine, bromine, and iodine (Cl, Br, and I, respectively), ammonia (NH3), and water (H2O). See also base; electrophile.


nucleophile [′nü·klē·ə‚fīl]
(physical chemistry)
A species possessing one or more electron-rich sites, such as an unshared pair of electrons, the negative end of a polar bond, or pi electrons. Also known as electron donor.


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5-7) The aim of this work was to prepare hyperbranched polyesters bearing amine groups of low nucleophilicity due to H-bonding.
Without study of the kinetics of polymerization, it is difficult to speak about the rate and rate constants of a reaction, nevertheless, it is reasonable to suppose that the nucleophilicity of phenol is the dominating force of this reaction.
Thus it is possibly established that the -OH group in aromatic linkages increases its degree of nucleophilicity, which in turn increases its linkage with the polymer.
 
 
 
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